Lipid Metabolism Disorders Diagnosis and Therapy: Challenges and Opportunities

A special issue of Metabolites (ISSN 2218-1989). This special issue belongs to the section "Lipid Metabolism".

Deadline for manuscript submissions: closed (30 March 2022) | Viewed by 25633

Special Issue Editors


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Guest Editor
Division of Medicine, University Medical Centre Ljubljana, 1000 Ljubljana, Slovenia
Interests: atherosclerosis; lipids; cardiovascular disease prevention; risk factors
Special Issues, Collections and Topics in MDPI journals
Department of Vascular Medicine, University Medical Centre Ljubljana, 1000 Ljubljana, Slovenia
Interests: atherosclerosis; lipids; cardiovascular disease prevention; risk factors
Special Issues, Collections and Topics in MDPI journals

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Guest Editor
Department of Internal Medicine and Medical Specialties (DIMIS), Università degli Studi di Palermo UNIPA, 90100 Palermo, Italy
Interests: cardiovascular risk; lipids; diabetes; prevention; therapy; metabolic syndrome; metabolism; lipoproteins; incretins; nutraceuticals
Special Issues, Collections and Topics in MDPI journals

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Guest Editor
1. School of Pharmacy and Biomolecular Sciences, Liverpool John Moores University, Liverpool L3 3AF, UK
2. Liverpool Centre for Cardiovascular Science, Liverpool L69 3BX, UK
Interests: cardiovascular; pharmacology

Special Issue Information

For nearly seven decades, dyslipidemia has been widely recognized as one of the most important risk factors for the development and complications of atherosclerotic cardiovascular disease (ASCVD). Large epidemiological and clinical trials have provided robust evidence in support of the fact that the magnitude of low-density lipoprotein cholesterol (LDL-C) lowering, in front of all by statins, consistently predicts the reduction of ASCVD risk.

However, several questions related to more comprehensive, higher-quality management of elevated LDL-C levels remain to be answered. These include more consistent use of the highest possible doses of potent statins, easier prescription of combination therapies, faster and better identification of patients with dyslipidemia who would benefit from alternative treatment strategies, such as PCSK9 inhibition, as well as the issue of diagnosis and effective management of statin intolerance and its subjective equivalents. Additionally, the question of when to start and how aggressively to treat hypercholesterolemia in children, adolescents, and the elderly, as well as whether to treat with statins the ASCVD risk itself in very-high- and high-risk patients with “normal” (low) LDL-C levels.

Despite the unequivocal efficiency of statins, the issue of residual ASCVD risk related to dyslipidemia remains, even in patients with already low LDL-C, such as the challenge of the best possible management of patients with combined (mixed) hyperlipidemia, atherogenic dyslipidemia (lipid triad), or moderate hypertriglyceridemia. We face these challenges in most patients with metabolic syndrome and diabetes mellitus, increasing in prevalence.

Furthermore, the role of the increased levels and the potential clinical efficiency of much more effective lowering of lipoprotein (a) is an increasingly challenging topic. Although our armamentarium of available pharmacologic interventions is fortunately expanding, further well-designed studies are needed to assess the clinical effectiveness and long-term safety of any of these new pharmacological options.

The majority of up-to-date preventive cardiology guidelines encompass numerous, increasingly evidence-supported recommendations on the way to approach the difficulties of poor compliance and adherence to long-term lipid-lowering therapy. Further, different aspects of dyslipidemia diagnosis and therapy in the era of contemporary, so-called “4P” (predictive, preemptive, personalized, and participatory) medicine are worth discussing, primarily the perspectives of a more efficient use of individual genetic information for both diagnostic and therapeutic purposes. In general, a more personalized but comprehensive approach is required instead of a “one size fits for all” intervention.

In summary, with this Special Issue of Metabolites, it is our aim to critically review available evidence on some of the above listed challenges that need to be met. We would prefer to discuss the best possible choices on the update of existing and on the development of novel lipid diagnostic and more effective pharmacotherapeutics to scale back the burden of ASCVD.

Prof. Dr. Zlatko Fras
Dr. Borut Jug
Prof. Dr. Manfredi Rizzo
Dr. Peter E. Penson
Guest Editors

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Published Papers (7 papers)

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Editorial

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5 pages, 187 KiB  
Editorial
Challenges and Opportunities on Lipid Metabolism Disorders Diagnosis and Therapy: Novel Insights and Future Perspective
by Zlatko Fras, Borut Jug, Peter E. Penson and Manfredi Rizzo
Metabolites 2021, 11(9), 611; https://doi.org/10.3390/metabo11090611 - 9 Sep 2021
Cited by 5 | Viewed by 2294
Abstract
Dyslipidemia has been globally recognized, for almost seven decades, as one of the most important risk factors for the development and complications of atherosclerotic cardiovascular disease (ASCVD) [...] Full article

Research

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11 pages, 1567 KiB  
Article
Proteinuria-Lowering Effects of Proprotein Convertase Subtilisin/Kexin Type 9 Inhibitors in Chronic Kidney Disease Patients: A Real-World Multicentric Study
by Patricia Muñoz Ramos, Yohana Gil Giraldo, Vicente Álvarez-Chiva, David Arroyo, Cristina Sango Merino, Francesc Moncho Francés, Javier Ocaña, Javier Reque, Emilio Sánchez-Álvarez, José Luis Górriz and Borja Quiroga
Metabolites 2021, 11(11), 760; https://doi.org/10.3390/metabo11110760 - 5 Nov 2021
Cited by 4 | Viewed by 2964
Abstract
Control of dyslipidemia in chronic kidney disease (CKD) is not always guaranteed with statins and/or ezetimibe. Proprotein convertase subtilisin/kexin type 9 inhibitors (PCSK9i) have opened up a new era in lipid control, but their effect on renal function and proteinuria in real life [...] Read more.
Control of dyslipidemia in chronic kidney disease (CKD) is not always guaranteed with statins and/or ezetimibe. Proprotein convertase subtilisin/kexin type 9 inhibitors (PCSK9i) have opened up a new era in lipid control, but their effect on renal function and proteinuria in real life have not yet been evaluated. The aim of the present study was to analyze the evolution of renal function and proteinuria in a cohort of CKD patients treated with PCSK9i. This retrospective multicentric cohort study included CKD patients treated with PCSK9i. Baseline epidemiological data, comorbidities and laboratory findings (including estimated glomerular filtration rate [eGFR], proteinuria and lipid profile) were collected. The evolution of renal function, proteinuria and lipid profile was analyzed during the 1-year follow-up. The cohort included 76 patients (68% male, mean age 66 ± 10 years). The mean baseline creatinine was 1.55 ± 0.77 mg/dL, and the mean eGFR was 52 ± 22 mL/min/1.73 m2. Reductions in LDL-cholesterol, total cholesterol and triglycerides during the first month were 51 ± 25%, 32 ± 25% and 11 ± 40%, respectively, levels that remained stable throughout the first year (p < 0.001 for LDL-cholesterol and total cholesterol trends and p = 0.002 for triglyceride trend). During follow-up, proteinuria improved from 57 (9–481) to 30 (7–520) mg/g (p = 0.021). In addition, eGFR remained stable, and no adverse events were reported. In our cohort, dyslipidemia treatment with PCSK9i was associated with decreased proteinuria in CKD patients, an effect that might be due to reduced lipid nephrotoxicity. Clinical trials are needed to further investigate whether this impact on proteinuria can significantly slow CKD progression in the long term. Full article
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9 pages, 645 KiB  
Article
Betatrophin Levels Are Related to the Early Histological Findings in Nonalcoholic Fatty Liver Disease
by Alper Sonmez, Teoman Dogru, Cemal Nuri Ercin, Halil Genc, Gurkan Celebi, Hasan Gurel, Serkan Tapan, Ali Fuat Cicek, Cem Barcin, Cem Haymana, Ali Kirik and Manfredi Rizzo
Metabolites 2021, 11(7), 425; https://doi.org/10.3390/metabo11070425 - 28 Jun 2021
Cited by 6 | Viewed by 2692
Abstract
Betatrophin, a liver hormone, regulates glucose and lipid metabolism. We investigated the betatrophin levels in nonalcoholic fatty liver disease (NAFLD) and searched for any relationship with histological severity and metabolic parameters. Fifty males with NAFLD [Nonalcoholic Steatohepatitis (NASH) (n = 32); non-NASH (n [...] Read more.
Betatrophin, a liver hormone, regulates glucose and lipid metabolism. We investigated the betatrophin levels in nonalcoholic fatty liver disease (NAFLD) and searched for any relationship with histological severity and metabolic parameters. Fifty males with NAFLD [Nonalcoholic Steatohepatitis (NASH) (n = 32); non-NASH (n = 18)] and 30 healthy controls were included. Plasma betatrophin was measured by ELISA method. Insulin sensitivity was assessed by HOMA-IR index. Histological features were scored by the semi quantitative classification and combined as the NAFLD activity score (NAS). Betatrophin levels in the non-NASH group were significantly higher than the controls. Betatrophin was positively correlated to the age, waist circumference, total cholesterol, triglycerides, LDL cholesterol, glucose, insulin, HOMA-IR index and gamma glutamyl transpeptidase levels, and negatively correlated to the steatosis and NAS. In the stepwise linear regression analysis, the triglyceride (β = 0.457, p < 0.001), glucose (β = 0.281, p = 0.02) and NAS (β = −0.260, p = 0.03) were the independent determinants of betatrophin. Betatrophin levels are higher in the early stages of NAFLD and tend to decrease when the disease progresses. This could be an important preliminary mechanistic finding to explain the increased frequency of glucose intolerance during the course of NAFLD. Full article
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14 pages, 1055 KiB  
Article
Preliminary Results of CitraVes™ Effects on Low Density Lipoprotein Cholesterol and Waist Circumference in Healthy Subjects after 12 Weeks: A Pilot Open-Label Study
by Stefania Raimondo, Dragana Nikolic, Alice Conigliaro, Gianluca Giavaresi, Bruna Lo Sasso, Rosaria Vincenza Giglio, Roberta Chianetta, Mauro Manno, Samuele Raccosta, Valeria Corleone, Giovanni Ferrante, Roberto Citarrella, Manfredi Rizzo, Giacomo De Leo, Marcello Ciaccio, Giuseppe Montalto and Riccardo Alessandro
Metabolites 2021, 11(5), 276; https://doi.org/10.3390/metabo11050276 - 27 Apr 2021
Cited by 21 | Viewed by 3294
Abstract
Appropriate monitoring and control of modifiable risk factors, such as the level of low-density lipoprotein cholesterol (LDL-C) and other types of dyslipidemia, have an important role in the prevention of cardiovascular diseases (CVD). Recently, various nutraceuticals with lipid-lowering effects have gained attention. In [...] Read more.
Appropriate monitoring and control of modifiable risk factors, such as the level of low-density lipoprotein cholesterol (LDL-C) and other types of dyslipidemia, have an important role in the prevention of cardiovascular diseases (CVD). Recently, various nutraceuticals with lipid-lowering effects have gained attention. In addition to the plant-derived bioactive compounds, recent studies suggested that plant cells are able to release small lipoproteic structures named extracellular vesicles (EVs). The interaction between EVs and mammalian cells could lead to beneficial effects through anti-inflammatory and antioxidant activities. The present study aimed to assess the safety of the new patented plant-based product citraVes™, containing extracellular vesicles (EVs) from Citrus limon (L.) Osbeck juice, and to investigate its ability to modulate different CV risk factors in healthy subjects. A cohort of 20 healthy volunteers was recruited in a prospective open-label study. All participants received the supplement in a spray-dried formulation at a stable dose of 1000 mg/day for 3 months. Anthropometric and hematobiochemical parameters were analyzed at the baseline and after the follow-up period of 1 and 3 months. We observed that the supplement has an effect on two key factors of cardiometabolic risk in healthy subjects. A significant change in waist circumference was found in women after 4 (85.4 [79.9, 91.0] cm, p < 0.005) and 12 (85.0 [80.0, 90.0] cm, p < 0.0005) weeks, when compared to the baseline value (87.6 [81.7, 93.6] cm). No difference was found in men (baseline: 100.3 [95.4, 105.2] cm; 4 weeks: 102.0 [95.7, 108.3] cm; 12 weeks: 100.0 [95.3, 104.7] cm). The level of LDL-C was significantly lower at 12 weeks versus 4 weeks (p = 0.0064). Our study evaluated, for the first time, the effects of a natural product containing plant-derived EVs on modifiable risk factors in healthy volunteers. The results support the use of EV extracts to manage cardiometabolic risk factors successfully. Full article
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Review

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31 pages, 3574 KiB  
Review
Severe Hypertriglyceridaemia and Chylomicronaemia Syndrome—Causes, Clinical Presentation, and Therapeutic Options
by Bilal Bashir, Jan H. Ho, Paul Downie, Paul Hamilton, Gordon Ferns, Dev Datta, Jaimini Cegla, Anthony S. Wierzbicki, Charlotte Dawson, Fiona Jenkinson, Hannah Delaney, Michael Mansfield, Yee Teoh, Zosia Miedzybrodzka, Haya Haso, Paul N. Durrington and Handrean Soran
Metabolites 2023, 13(5), 621; https://doi.org/10.3390/metabo13050621 - 30 Apr 2023
Cited by 12 | Viewed by 4480
Abstract
We have reviewed the genetic basis of chylomicronaemia, the difference between monogenic and polygenic hypertriglyceridaemia, its effects on pancreatic, cardiovascular, and microvascular complications, and current and potential future pharmacotherapies. Severe hypertriglyceridaemia (TG > 10 mmol/L or 1000 mg/dL) is rare with a prevalence [...] Read more.
We have reviewed the genetic basis of chylomicronaemia, the difference between monogenic and polygenic hypertriglyceridaemia, its effects on pancreatic, cardiovascular, and microvascular complications, and current and potential future pharmacotherapies. Severe hypertriglyceridaemia (TG > 10 mmol/L or 1000 mg/dL) is rare with a prevalence of <1%. It has a complex genetic basis. In some individuals, the inheritance of a single rare variant with a large effect size leads to severe hypertriglyceridaemia and fasting chylomicronaemia of monogenic origin, termed as familial chylomicronaemia syndrome (FCS). Alternatively, the accumulation of multiple low-effect variants causes polygenic hypertriglyceridaemia, which increases the tendency to develop fasting chylomicronaemia in presence of acquired factors, termed as multifactorial chylomicronaemia syndrome (MCS). FCS is an autosomal recessive disease characterized by a pathogenic variant of the lipoprotein lipase (LPL) gene or one of its regulators. The risk of pancreatic complications and associated morbidity and mortality are higher in FCS than in MCS. FCS has a more favourable cardiometabolic profile and a low prevalence of atherosclerotic cardiovascular disease (ASCVD) compared to MCS. The cornerstone of the management of severe hypertriglyceridaemia is a very-low-fat diet. FCS does not respond to traditional lipid-lowering therapies. Several novel pharmacotherapeutic agents are in various phases of development. Data on the correlation between genotype and phenotype in FCS are scarce. Further research to investigate the impact of individual gene variants on the natural history of the disease, and its link with ASCVD, microvascular disease, and acute or recurrent pancreatitis, is warranted. Volanesorsen reduces triglyceride concentration and frequency of pancreatitis effectively in patients with FCS and MCS. Several other therapeutic agents are in development. Understanding the natural history of FCS and MCS is necessary to rationalise healthcare resources and decide when to deploy these high-cost low-volume therapeutic agents. Full article
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22 pages, 1118 KiB  
Review
Metabolomics of Arterial Stiffness
by Kaido Paapstel and Jaak Kals
Metabolites 2022, 12(5), 370; https://doi.org/10.3390/metabo12050370 - 20 Apr 2022
Cited by 14 | Viewed by 3660
Abstract
Arterial stiffness (AS) is one of the earliest detectable signs of structural and functional alterations of the vessel wall and an independent predictor of cardiovascular events and death. The emerging field of metabolomics can be utilized to detect a wide spectrum of intermediates [...] Read more.
Arterial stiffness (AS) is one of the earliest detectable signs of structural and functional alterations of the vessel wall and an independent predictor of cardiovascular events and death. The emerging field of metabolomics can be utilized to detect a wide spectrum of intermediates and products of metabolism in body fluids that can be involved in the pathogenesis of AS. Research over the past decade has reinforced this idea by linking AS to circulating acylcarnitines, glycerophospholipids, sphingolipids, and amino acids, among other metabolite species. Some of these metabolites influence AS through traditional cardiovascular risk factors (e.g., high blood pressure, high blood cholesterol, diabetes, smoking), while others seem to act independently through both known and unknown pathophysiological mechanisms. We propose the term ‘arteriometabolomics’ to indicate the research that applies metabolomics methods to study AS. The ‘arteriometabolomics’ approach has the potential to allow more personalized cardiovascular risk stratification, disease monitoring, and treatment selection. One of its major goals is to uncover the causal metabolic pathways of AS. Such pathways could represent valuable treatment targets in vascular ageing. Full article
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14 pages, 1119 KiB  
Review
CRISPR Gene Editing in Lipid Disorders and Atherosclerosis: Mechanisms and Opportunities
by Harry E. Walker, Manfredi Rizzo, Zlatko Fras, Borut Jug, Maciej Banach and Peter E. Penson
Metabolites 2021, 11(12), 857; https://doi.org/10.3390/metabo11120857 - 9 Dec 2021
Cited by 14 | Viewed by 4429
Abstract
Elevated circulating concentrations of low-density lipoprotein cholesterol (LDL-C) have been conclusively demonstrated in epidemiological and intervention studies to be causally associated with the development of atherosclerotic cardiovascular disease. Enormous advances in LDL-C reduction have been achieved through the use of statins, and in [...] Read more.
Elevated circulating concentrations of low-density lipoprotein cholesterol (LDL-C) have been conclusively demonstrated in epidemiological and intervention studies to be causally associated with the development of atherosclerotic cardiovascular disease. Enormous advances in LDL-C reduction have been achieved through the use of statins, and in recent years, through drugs targeting proprotein convertase subtilisin/kexin type 9 (PCSK9), a key regulator of the hepatic LDL-receptor. Existing approaches to PCSK9 targeting have used monoclonal antibodies or RNA interference. Although these approaches do not require daily dosing, as statins do, repeated subcutaneous injections are nevertheless necessary to maintain effectiveness over time. Recent experimental studies suggest that clustered regularly interspaced short palindromic repeats (CRISPR) gene-editing targeted at PCSK9 may represent a promising tool to achieve the elusive goal of a ‘fire and forget’ lifelong approach to LDL-C reduction. This paper will provide an overview of CRISPR technology, with a particular focus on recent studies with relevance to its potential use in atherosclerotic cardiovascular disease. Full article
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